Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease

Objectives: The objective of this study was to evaluate muscular metabolic function in children with inactive juvenile idiopathic arthritis (JIA).Methods: Fifteen children with inactive JIA and fifteen healthy controls were matched by sex, biological age, and Tanner stage. Participants completed a s...

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Main Authors: Emmanuelle Rochette, Pierre Bourdier, Bruno Pereira, Stéphane Echaubard, Corinne Borderon, Nicolas Caron, Aurélie Chausset, Daniel Courteix, Solenne Fel, Justyna Kanold, Justine Paysal, Sébastien Ratel, Nadège Rouel, Catherine Sarret, Daniel Terral, Alexandra Usclade, Etienne Merlin, Pascale Duché
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-05-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphys.2019.00528/full
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author Emmanuelle Rochette
Emmanuelle Rochette
Emmanuelle Rochette
Emmanuelle Rochette
Pierre Bourdier
Bruno Pereira
Stéphane Echaubard
Stéphane Echaubard
Corinne Borderon
Nicolas Caron
Aurélie Chausset
Aurélie Chausset
Daniel Courteix
Solenne Fel
Justyna Kanold
Justyna Kanold
Justine Paysal
Sébastien Ratel
Nadège Rouel
Nadège Rouel
Catherine Sarret
Catherine Sarret
Daniel Terral
Alexandra Usclade
Alexandra Usclade
Etienne Merlin
Etienne Merlin
Etienne Merlin
Pascale Duché
Pascale Duché
Pascale Duché
spellingShingle Emmanuelle Rochette
Emmanuelle Rochette
Emmanuelle Rochette
Emmanuelle Rochette
Pierre Bourdier
Bruno Pereira
Stéphane Echaubard
Stéphane Echaubard
Corinne Borderon
Nicolas Caron
Aurélie Chausset
Aurélie Chausset
Daniel Courteix
Solenne Fel
Justyna Kanold
Justyna Kanold
Justine Paysal
Sébastien Ratel
Nadège Rouel
Nadège Rouel
Catherine Sarret
Catherine Sarret
Daniel Terral
Alexandra Usclade
Alexandra Usclade
Etienne Merlin
Etienne Merlin
Etienne Merlin
Pascale Duché
Pascale Duché
Pascale Duché
Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease
Frontiers in Physiology
pediatric
physical activity
inflammation
fat oxidation
metabolism
author_facet Emmanuelle Rochette
Emmanuelle Rochette
Emmanuelle Rochette
Emmanuelle Rochette
Pierre Bourdier
Bruno Pereira
Stéphane Echaubard
Stéphane Echaubard
Corinne Borderon
Nicolas Caron
Aurélie Chausset
Aurélie Chausset
Daniel Courteix
Solenne Fel
Justyna Kanold
Justyna Kanold
Justine Paysal
Sébastien Ratel
Nadège Rouel
Nadège Rouel
Catherine Sarret
Catherine Sarret
Daniel Terral
Alexandra Usclade
Alexandra Usclade
Etienne Merlin
Etienne Merlin
Etienne Merlin
Pascale Duché
Pascale Duché
Pascale Duché
author_sort Emmanuelle Rochette
title Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease
title_short Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease
title_full Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease
title_fullStr Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease
title_full_unstemmed Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease
title_sort impaired muscular fat metabolism in juvenile idiopathic arthritis in inactive disease
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2019-05-01
description Objectives: The objective of this study was to evaluate muscular metabolic function in children with inactive juvenile idiopathic arthritis (JIA).Methods: Fifteen children with inactive JIA and fifteen healthy controls were matched by sex, biological age, and Tanner stage. Participants completed a submaximal incremental exercise test to determine their fat and carbohydrate oxidation rates.Results: Between the two groups, heart rate values and carbohydrate oxidation rates were the same, regardless of the relative intensity of exercise. Lipid oxidation rates were lower in JIA patients, regardless of the percentage of VO2 peak (p < 0.05). Respiratory exchange ratios beyond 50% of VO2 peak were higher in patients with JIA (p < 0.05). Respective maximal fat oxidation rates (MFO) for controls and children with JIA were 218.7 ± 92.2 vs. 157.5 ± 65.9 mg ⋅ min-1 (p = 0.03) and 4.9 ± 1.9 vs. 3.4 ± 1.2 mg ⋅ min-1 ⋅ kg-1 (p = 0.04). There was no difference between the two groups in heart rate, percentage of VO2 peak, or power of exercise to achieve MFO. Controls reached their MFO at an exercise power significantly higher than did JIA subjects (42.8 ± 16.8 and 31.9 ± 9.8 W, p = 0.004).Conclusion: Children with JIA show metabolic disturbance during exercise, even when the disease is considered inactive. This disturbance is seen in a lower lipid oxidation rate during submaximal exercise.
topic pediatric
physical activity
inflammation
fat oxidation
metabolism
url https://www.frontiersin.org/article/10.3389/fphys.2019.00528/full
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spelling doaj-5a61269328fc4a56914faf8de7e0941a2020-11-25T00:43:27ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2019-05-011010.3389/fphys.2019.00528435098Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive DiseaseEmmanuelle Rochette0Emmanuelle Rochette1Emmanuelle Rochette2Emmanuelle Rochette3Pierre Bourdier4Bruno Pereira5Stéphane Echaubard6Stéphane Echaubard7Corinne Borderon8Nicolas Caron9Aurélie Chausset10Aurélie Chausset11Daniel Courteix12Solenne Fel13Justyna Kanold14Justyna Kanold15Justine Paysal16Sébastien Ratel17Nadège Rouel18Nadège Rouel19Catherine Sarret20Catherine Sarret21Daniel Terral22Alexandra Usclade23Alexandra Usclade24Etienne Merlin25Etienne Merlin26Etienne Merlin27Pascale Duché28Pascale Duché29Pascale Duché30Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre de Recherche en Nutrition Humaine d’Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceDélégation à la Recherche Clinique et à l‘Innovation, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceINRA, UMR 1019 UNH, ECREIN, Université Clermont Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre de Recherche en Nutrition Humaine d’Auvergne, Clermont-Ferrand, FranceLaboratoire Impact de l’Activité Physique sur la Santé, Université de Toulon, Toulon, FranceObjectives: The objective of this study was to evaluate muscular metabolic function in children with inactive juvenile idiopathic arthritis (JIA).Methods: Fifteen children with inactive JIA and fifteen healthy controls were matched by sex, biological age, and Tanner stage. Participants completed a submaximal incremental exercise test to determine their fat and carbohydrate oxidation rates.Results: Between the two groups, heart rate values and carbohydrate oxidation rates were the same, regardless of the relative intensity of exercise. Lipid oxidation rates were lower in JIA patients, regardless of the percentage of VO2 peak (p < 0.05). Respiratory exchange ratios beyond 50% of VO2 peak were higher in patients with JIA (p < 0.05). Respective maximal fat oxidation rates (MFO) for controls and children with JIA were 218.7 ± 92.2 vs. 157.5 ± 65.9 mg ⋅ min-1 (p = 0.03) and 4.9 ± 1.9 vs. 3.4 ± 1.2 mg ⋅ min-1 ⋅ kg-1 (p = 0.04). There was no difference between the two groups in heart rate, percentage of VO2 peak, or power of exercise to achieve MFO. Controls reached their MFO at an exercise power significantly higher than did JIA subjects (42.8 ± 16.8 and 31.9 ± 9.8 W, p = 0.004).Conclusion: Children with JIA show metabolic disturbance during exercise, even when the disease is considered inactive. This disturbance is seen in a lower lipid oxidation rate during submaximal exercise.https://www.frontiersin.org/article/10.3389/fphys.2019.00528/fullpediatricphysical activityinflammationfat oxidationmetabolism